Validation Specialist Jobs

RSS

46 Validation Specialist jobs found on Monster.

Jobs 1 to 20 of 46
Company Confidential Amityville, NY, 11701
VALIDATION SPECIALIST –CLEANING QUALIFICATION Our Company We are a rapidly growing pharmaceutical manufacturer, with core competencies in the sterile injectable and ophthalmic sectors, and with many new products in development and awaiting FDA approval. In anticipation of long-term, substantial growth, we offer challenging, attractive career opportunities along with competitive salaries and comp...
They have a large lab, the person who is the validation specialist will be watching all of the blending of product and filling of bottles. After the product is blended they will obtain samples and have the samples tested. They will analyze the data and fill out reports. Must be able to follow steps precisely. Must write everything down, they will write up reports after the blending and testing pro...
Validation Specialist to lead automation qualification activities throughout the site on multiple automation platforms including PLC’s, DeltaV Distributed Control Systems, Andover Building Automation Systems, and other automation platforms as implemented on site. Qualification of automation includes all areas of the manufacturing operations, site GMP utilities, and support of capital projects. Thi...
We are looking for an experienced validation individual who can help a consumer pharmaceutical with validation life cycle activities. This individual would be working on developing validation master plan, equipment qualifications and process validations (cleaning validation and packaging process) for new product. This position currently slated for 6 months but has a high potential of being long te...
Church & Dwight Co Inc York, PA
Information about this job: Overview: General Summary: This position will be responsible for performing validation of equipment and processes for the manufacturing and packaging operations. This includes, but is not limited to, identifying equipment and / or processes, preparing IQ (Installation Qualification) / OQ (Operational Qualification) / PQ (Production Qualification) protocols, performin...
Thermo Fisher Bedford, OH
Expertise Quality Assurance Education Bachelors Job Type Full-time Location United States - Ohio - Oakwood Village Job Level Experienced Posting date: August 12, 2014 Position Summary: Responsible for establishing a high degree of assurance that new/modified medical device hardware and software products for use in scientific industries have been fully validated, such that they will perform cons...
Thermo Fisher Rockville, MD
Expertise Information Technology Job Type Full-time Location United States - Maryland - Rockville Job Level Experienced Posting date: August 21, 2014 Position Summary : This position will be required to manage various software validation efforts throughout the company. This person will be viewed as the internal expert with regard to the FDA regulation 21 CFR Part 11. Key Responsibilities: % 1...
Description CSC has an immediate position for a Computer Validation Specialist within the DOC Systems group. This position is located in Frederick, Maryland. Essential Job Functions Ensure IT infrastructure, hardware and software systems purchased by DVC for the regulated network are installed, perform and operate according to specifications and user requirements. Lead qualification and valida...
Join STERIS in its vision to see the world free from Infection and Contamination as a Validation Specialist III Position Summary: Develops, executes, and prepares final reports of validation/qualification studies of sterilization ,cleaning, manufacturing, software and laboratory processes, supports the design and establishment of Quality Service systems such as Steam, Water, Air and Controlled ...
Overview: Validation Specialist to lead automation qualification activities throughout the site on multiple automation platforms including PLC’s, DeltaV Distributed Control Systems, Andover Building Automation Systems, and other automation platforms as implemented on site. Qualification of automation includes all areas of the manufacturing operations, site GMP utilities, and support of capital pr...
Overview: Responsible for developing and validating release, in-process and cleaning methods in support of Novartis Diagnostic’s immunodiagnostic products. This role will interact with Technology Development, Manufacturing, Research & Development, Quality Control and Quality Assurance staff to ensure that method validation and transfer studies are appropriate for the methods’ intended use(s) and ...
Arizona's Children Association Tucson, AZ, 85704
GENERAL POSITION SUMMARY: The Data Validation Specialist is responsible for conducting internal billing and medical records audits, and the provision of training and technical assistance of behavioral health coding and billing activities. The position reviews billing and coding data and documentation in the electronic health record to determine accuracy, quality and timeliness. The Data Validatio...
Grifols, Inc. Emeryville, CA
Overview: Responsible for developing and validating release, in-process and cleaning methods in support of Novartis Diagnostic’s immunodiagnostic products. This role will interact with Technology Development, Manufacturing, Research & Development, Quality Control and Quality Assurance staff to ensure that method validation and transfer studies are appropriate for the methods’ intended use(s) and ...
Validation Specialist-Data Applications Job ID GBS-0681780 Job type Full-time Complementary Work country USA Position type Professional Work city Indianapolis,IN Posted 04-Aug-2014 Travel Unknown at this time Job area Consulting & Services Business group Global Business Services Job category IT Specialist Business unit AS Job role Business Analyst Job role skillset Application Development P...
Title/Position Computer Systems Validation Specialist-Serialization Location Yardley, PA Description Xyntek is seeking entrepreneurial-minded, dedicated and motivated employees that are interested in joining a fast-paced Systems Engineering & Consulting Team. The ideal candidates will be involved in all aspects of computer systems validation and qualification activities as part of an overall ...
Step 7 Atlanta, GA
ProGXP is seeking a Lab Validation Engineer to develop and design the validation plans and testing protocols for blood transfusion and blood transplant diagnostic equipment, as well as execute test plans. Our client is a fast-paced organization with extremely high quality and regulatory standards. Efficiency and accuracy, as well as the ability to improve processes and innovate, are essential to s...
Thermo Fisher Scientific Inc. Rockville, MD, 20850
Posting date: August 21, 2014 Position Summary : This position will be required to manage various software validation efforts throughout the company. This person will be viewed as the internal expert with regard to the FDA regulation 21 CFR Part 11. Key Responsibilities: % 1. Interpret and apply government regulations, guidance documents, and industry standards pertaining to the validation an...
University of Pennsylvania Philadelphia, PA, 19107
The Quality Systems Validation Specialist will support the successful operation of the Clinical Cell and Vaccine Production Facility ( CVPF ) at the University of Pennsylvania to manufacture cell and gene therapy products for early phase I clinical trials in HIV and cancer. The Quality Systems Validation Specialist will serve as a liaison across multiple functional groups within the CVPF , includi...
If you have experience performing software testing along with reviewing client requirements and specifications, learn more about how you can be a part of growing Clinical Research Organization that offers continued growth in the field of Technology. About the Validation Specialist role within ICON: The Validation Specialist will execute formal test scripts, complete associated documentation and ...
Global Employment Solutions Inc. Appleton, WI
Job Description: We are hiring for a Validation Specialist to work in the Automation Quality System capacity for a global leader in pharmaceutical development and manufacturing company. SUMMARY: Individual will generate protocols, execute protocols and generate final reports to support the qualification / validation of PLC, SCADA, PC and other controls based systems. The individual will be expe...

Get new jobs by email for this search
We'll keep looking and send you new jobs that match this search.
email me

Upload your resume and let employers find you!
It's that simple!

Engineering Career Tools

Regulations Compliance Associate

Salaries

$31,200.00 - $94,080.00
Typical Salary for Regulations Compliance Associate
(53 Respondents)
Source: Monster.com Careerbenchmarking Tool

Education / Training

Bachelor's
46.9%
Master's
18.4%
Some College Coursework Completed
12.2%
Associates
6.1%
Doctorate
6.1%
Professional
6.1%
High School
4.1%
(49 Respondents)
Source: Monster.com Careerbenchmarking Tool

Popular Validation Specialist Articles

Eight Bright-Outlook Careers Article Rating
What are tomorrow's jobs today? Check out eight careers identified by O*Net as having some of the strongest job prospects in the coming years.
Sample Resume for a Midlevel Clinical Data Specialist Article Rating
Data management is crucial to career -- and resume -- success. This clinical data specialist resume shows the right amount of information to highlight.
For Employers: Post Jobs | Search Resumes | Advertise
About Monster | Work for Monster | Advertise with Us | AdChoices | Partner with Us | Investor Relations | Social Media
Terms of Use | Privacy Center | Accessibility Center | Help | Security | Contact Us | Sitemap | Mobile
©2014 Monster - All Rights Reserved U.S. Patents No. 5,832,497; 7,599,930 B1; 7,827,125 and 7,836,060 MWW - Looking for Monster Cable? - V: 2014.4.45.50-314
eTrustLogo